Canonical Allele Identifier: CA368056996

Gene: ABCB4

Linked Data

• MyVariant Identifiers: chr7:g.87031575C>G (hg19) ; chr7:g.87402259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87402259C>G , CM000669.2:g.87402259C>G	GRCh38
NC_000007.13:g.87031575C>G , CM000669.1:g.87031575C>G	GRCh37
NC_000007.12:g.86869511C>G	NCBI36
NG_007118.1:g.83174G>C
NG_007118.2:g.83174G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359206.8:c.3677G>C	ENSP00000352135.3:p.Cys1226Ser
ENST00000649586.2:c.3677G>C MANE Select	ENSP00000496956.2:p.Cys1226Ser
ENST00000265723.8:c.3698G>C	ENSP00000265723.4:p.Cys1233Ser
ENST00000358400.7:c.3536G>C	ENSP00000351172.3:p.Cys1179Ser
ENST00000359206.7:c.3677G>C	ENSP00000352135.3:p.Cys1226Ser
ENST00000440025.1:c.111G>C
ENST00000453593.5:c.3536G>C	ENSP00000392983.1:p.Cys1179Ser
ENST00000467983.1:n.289G>C
NM_000443.3:c.3677G>C	NP_000434.1:p.Cys1226Ser
NM_018849.2:c.3698G>C	NP_061337.1:p.Cys1233Ser
NM_018850.2:c.3536G>C	NP_061338.1:p.Cys1179Ser
XM_011516308.1:c.3698G>C	XP_011514610.1:p.Cys1233Ser
XM_011516309.1:c.3677G>C	XP_011514611.1:p.Cys1226Ser
XM_011516310.1:c.3593G>C	XP_011514612.1:p.Cys1198Ser
XM_011516311.1:c.3569G>C	XP_011514613.1:p.Cys1190Ser
XM_011516312.1:c.3557G>C	XP_011514614.1:p.Cys1186Ser
XM_011516313.1:c.3536G>C	XP_011514615.1:p.Cys1179Ser
XM_011516314.1:c.3719G>C	XP_011514616.1:p.Cys1240Ser
XM_011516315.1:c.3038G>C	XP_011514617.1:p.Cys1013Ser
XM_011516308.3:c.3968G>C	XP_011514610.3:p.Cys1323Ser
XM_011516309.3:c.3947G>C	XP_011514611.3:p.Cys1316Ser
XM_011516310.3:c.3863G>C	XP_011514612.3:p.Cys1288Ser
XM_011516311.3:c.3839G>C	XP_011514613.3:p.Cys1280Ser
XM_011516312.3:c.3827G>C	XP_011514614.3:p.Cys1276Ser
XM_011516313.3:c.3806G>C	XP_011514615.2:p.Cys1269Ser
XM_011516315.3:c.3038G>C	XP_011514617.2:p.Cys1013Ser
XM_017012323.2:c.3698G>C	XP_016867812.1:p.Cys1233Ser
XR_001744809.2:n.4206G>C
NM_000443.4:c.3677G>C MANE Select	NP_000434.1:p.Cys1226Ser
NM_018849.3:c.3698G>C	NP_061337.1:p.Cys1233Ser
NM_018850.3:c.3536G>C	NP_061338.1:p.Cys1179Ser